Difference between revisions of "Part:BBa K1154000:Design"
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===Design Notes=== | ===Design Notes=== | ||
− | This commercially synthesized construct was designed for high codon bias in ''Saccharomyces cerevisiae'' and conformity with current Registry standards. Its component sequences can be found in the Registry (see Source) | + | This commercially synthesized construct was designed for high codon bias in ''Saccharomyces cerevisiae'' and conformity with current Registry standards. Its component sequences can be found in the Registry (see Source). |
===Source=== | ===Source=== |
Revision as of 11:51, 20 September 2013
Mating pheromone-induced IGPD and constitutive LDH expression in Yeast
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 763
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
This commercially synthesized construct was designed for high codon bias in Saccharomyces cerevisiae and conformity with current Registry standards. Its component sequences can be found in the Registry (see Source).
Source
This sequence was commercially synthesized. Component sequences can be found in the Registry: Yeast FUS1 promoter (BBa_K1154001); Yeast TEF2 promoter (BBa_K165037); Yeast ADH1 terminator (BBa_J63002); Yeast imidazoleglycerol-phosphate dehydratase (IGPD) coding sequence (BBa_K1154002); Human lactate dehydrogenase A (LDHA) coding sequence (BBa_K1154003). However, assembling these sequences using the Composite Parts Tool will not produce a sequence identical to the one submitted here.